Research Analyst

Title : Research Analyst II (Analytical Compliance Specialist)Length of Contract : 12 monthsLocation/Site : North Chicago, IL -Hybrid Onsite Schedule (3 days/week)What are the top 3-5 skills, experience or education required for this position:-.Preferred Qualifications Experience:-Experience supporting stability programs or quality control operationsExperience with instrument qualification, calibration, and maintenance coordinationExperience working with outsourced testing laboratories or external partnersFamiliarity with analytical testing workflows in a regulated environmentAnalytical Compliance Specialist-We are seeking an Analytical Scientist to support a variety of laboratory and quality-related activities. This role will play an important part in ensuring smooth laboratory operations, supporting compliance expectations, and coordinating analytical activities across internal and external partners.The ideal candidate will have experience in analytical chemistry and a strong background in quality systems, including GMP. This position requires excellent organizational skills, attention to detail, and the ability to collaborate effectively across functions.Key Responsibilities:Responsibilities may include:Support quality control coordination for drug substance and drug product stability programs including managing studies in LIMS• Assist with shipment coordination for samples and materials as needed• Provide laboratory instrument service documentation support for: calibration, qualification, maintenance, and repair• Assist in managing outsourced analytical testing activities and vendor interactions• Partner with subject matter experts to help coordinate routine and non-routine analytical tasks• Support troubleshooting, tracking, and follow-up of laboratory and quality-related issues• Ensure work is performed in alignment with GMP and applicable quality system requirements• Help maintain accurate records, reports, and documentationRequired Qualifications:• B.S. or M.S. degree in chemistry, biochemistry, pharmaceutical sciences, or a related scientific discipline• Experience in pharmaceutical in pharmaceutical and analytical development is desirable• Experience working within quality systems, including GMP, is required• Strong organizational and communication skills• Ability to manage multiple priorities and work collaboratively with cross-functional teams• Strong attention to detail and commitment to data integrity and complianceEEO: “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”